- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Executive Director , Head of Center of Excellence (CoE), Global Medical Safety ... various regions, offering guidance and support to each product safety team in critical areas such as individual case...expectedness of the adverse event in relation to the drug . Ensure all relevant data and findings are incorporated… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality ... possesses advanced knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and relevant regulatory… more
- Sumitomo Pharma (Trenton, NJ)
- …English. **Education and Experience** + **Medical Degree (MD) with 3-5 years of drug safety experience in a pharmaceutical company** + Experience in oncology ... Evaluation and Mitigation Strategy (REMS) + Contributes to PVRM and cross-functional drug development teams and manages Safety Charters + Handles Health… more
- Ascendis Pharma (Princeton, NJ)
- …2 days remote. Key Responsibilities + Assists Head of GPS Medical Science for drug safety and pharmacovigilance activities for ensuring corporate compliance ... for employees to grow and develop their skills. Associate Director , Global Patient Safety Medical Science reports...product safety . + Supports the development of safety surveillance and risk management plans for drug… more
- United Therapeutics (Trenton, NJ)
- …enjoy being part of a collaborative team. The Associate Global PV Case Management Director plays a key role in management and oversight of end-to-end case safety ... to ensure compliance with global regulations and guidelines with regards to safety data collection, management and reporting for postmarketing ICSRs for efficiency,… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …+ Resolves safety or relevant clinical issues in consultation with Global Drug Safety and Pharmacovigilance , SVP Late Clinical Development and the ... Director Clinical Development - Respiratory Date: May 28,...closely with other functional areas such as commercial, regulatory, pharmacovigilance , CMC, early clinical and pre-clinical development in this… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary** The Executive Director , Head of Center of Excellence (CoE), Global Medical Safety ... various regions, offering guidance and support to each product safety team in critical areas such as individual case...expectedness of the adverse event in relation to the drug . Ensure all relevant data and findings are incorporated… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality ... possesses advanced knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and relevant regulatory… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director , Ophthalmology **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ready to shape the future of ... medicine? The race is on to speed up drug discovery and development to find answers for patients...helping our teams accelerate progress. The Senior Clinical Research Director (CRD) is an **expert clinical lead for one… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …+ Ensuring alignment amongst relevant functional groups + Review of report from Drug Safety / Pharmacovigilance , as needed + Preparing for and participating ... depression in adults as monotherapy and as adjunctive therapy. The Senior Director , Medical Affairs supports the Medical Affairs department in the development and… more
